CELLINI, ELENA
 Distribuzione geografica
Continente #
NA - Nord America 2.586
EU - Europa 1.102
AS - Asia 226
AF - Africa 7
OC - Oceania 1
SA - Sud America 1
Totale 3.923
Nazione #
US - Stati Uniti d'America 2.582
PL - Polonia 278
SE - Svezia 213
IE - Irlanda 171
IT - Italia 145
CN - Cina 95
UA - Ucraina 94
DE - Germania 93
HK - Hong Kong 79
FI - Finlandia 44
GB - Regno Unito 37
TR - Turchia 22
JO - Giordania 12
SG - Singapore 9
CH - Svizzera 7
FR - Francia 7
SC - Seychelles 6
VN - Vietnam 6
RU - Federazione Russa 5
BE - Belgio 4
CA - Canada 4
KR - Corea 2
BG - Bulgaria 1
BR - Brasile 1
IL - Israele 1
LI - Liechtenstein 1
MK - Macedonia 1
MU - Mauritius 1
NL - Olanda 1
NZ - Nuova Zelanda 1
Totale 3.923
Città #
Fairfield 430
Warsaw 278
Chandler 243
Woodbridge 204
Cambridge 182
Ashburn 179
Dublin 170
Seattle 160
Jacksonville 159
Houston 158
Wilmington 131
Dearborn 94
Altamura 91
Ann Arbor 75
Lawrence 72
Buffalo 49
Princeton 49
Boardman 44
Hong Kong 44
Beijing 43
Medford 32
Boston 28
San Diego 25
Bremen 22
Izmir 22
Hefei 11
Florence 10
Norwalk 10
Shanghai 9
Frankfurt Am Main 8
Auburn Hills 7
Bern 7
Hillsboro 7
Kent 7
London 7
Los Angeles 7
Nanjing 5
Singapore 5
Brussels 4
Dong Ket 4
Guangzhou 4
Milan 4
New York 4
Toronto 4
Verona 4
Andover 3
Kunming 3
Old Bridge 3
Rome 3
Bari 2
Jiaxing 2
Moscow 2
Nanchang 2
Prescot 2
Seoul 2
Serra 2
Wandsworth 2
Wuhan 2
Acton 1
Arnsberg 1
Birmingham 1
Bologna 1
Catania 1
Central 1
Chiswick 1
Christchurch 1
Edinburgh 1
Fuzhou 1
Hangzhou 1
Harbin 1
Harleysville 1
Hebei 1
Hounslow 1
Huzhou 1
Messina 1
Naas 1
Nanning 1
Phoenix 1
Rancho Cucamonga 1
Redwood City 1
Saint Petersburg 1
San Mateo 1
Shenyang 1
Shenzhen 1
Skopje 1
Sofia 1
Stia 1
Tel Aviv 1
Tianjin 1
Vitória 1
Wenzhou 1
Totale 3.175
Nome #
Fat Mass and Obesity-Associated Gene (FTO) in Eating Disorders: Evidence for Association of the rs9939609 Obesity Risk Allele with Bulimia nervosa and Anorexia nervosa 225
Membrane cholesterol enrichment prevents Abeta-induced oxidative stress in Alzheimer's fibroblasts. 186
Clinical features and outcome of 6 new patients carrying de novoKCNB1gene mutations 110
Association analysis of the paraoxonase-1 gene with Alzheimer's disease 109
A2 macroglobulin polymorphisms in Italian sporadic and familial Alzheimer’s disease 102
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. 97
Fragile X premutation with atypical symptoms at onset. 95
Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits. 94
Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders. 94
Association of IL10 promoter polymorphism in Italian Alzheimer's disease. 94
Associations of individual and family eating patterns during childhood and early adolescence: a multicentre European study of associated eating disorder factors. 93
Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa. 92
Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians. 92
Lack of association between NOS3 poly morphism and Italian sporadic and familial Alzheimer's disease. 91
Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease. 90
Insulin degrading enzyme and alpha-3 catenin polymorphisms in italian patients with Alzheimer disease 89
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease 89
Present and lifetime comorbidity of tobacco, alcohol and drug use in eating disorders: a European multicenter study. 89
Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease. 89
Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa. 89
Lack of association between the CYP46 gene polymorphism and Italian late-onset sporadic Alzheimer's disease 88
Acylphosphatase expression during macrophage differentiation and activation of U-937 cell line 86
Identification of new presenilin gene mutations in early-onset familial Alzheimer disease 83
Atypical Friedreich ataxia with a very late onset and an unusual limited GAA repeat. 83
KIBRA gene variants are associated with episodic memory performance in subjective memory complaints. 82
Glucocorticoid receptor gene polymorphisms in Italian patients with eating disorders and obesity. 82
No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy. 81
Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease. 80
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity 80
Brain-derived neurotrophic factor genetic variants are notsusceptibility factors to Alzheimer's disease in Italy. 78
Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease. 75
Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia 74
Brain metabolic differences between sporadic and familial Alzheimer's disease. 72
Psychopathological traits and 5-HT2A receptor promoter polymorphism (-1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa. 72
Role of the neurotrophin network in eating disorders' subphenotypes: Body mass index and age at onset of the disease 70
Implication of sex and SORL1 variants in italian patients with Alzheimer disease. 70
Factors of risk and maintenance for eating disorders: psychometric exploration of the cross-cultural questionnaire(CCQ) across five European countries. 69
Cystatin C and apoe polymorphisms in Italian Alzheimer'sdisease. 67
Meta-analysis of the association between variants in SORL1 and Alzheimer disease. 63
Low social interactions in eating disorder patients in childhood and adulthood: A multi-centre European case control study. 57
Implication of GAB2 Gene Polymorphism in Italian Patients with Alzheimer's Disease 54
Mutational screening analysis of DHCR24/seladin-1 gene in Italian familial Alzheimer's disease. 52
Genetic Analysis of familial and sporadic cases of spinocerebellar ataxias in Italian patients 47
Lack of association between TNF-alpha polymorphisms and Alzheimer's disease in an Italian cohort 46
Testing for linkage and association across thedihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations. 43
Clinical and genetic analysis of a Machado-Joseph Italian family 33
Whole Exome Sequencing Is the Minimal Technological Approach in Probands Born to Consanguineous Couples 25
Distinct epilepsy phenotypes and response to drugs in KCNA1 gain- and loss-of function variants 21
Genetic and clinical analysis of SCA8 repeat expansion 20
Totale 3.962
Categoria #
all - tutte 10.974
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 10.974


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019359 0 0 0 0 0 0 0 0 0 0 196 163
2019/20201.056 89 60 25 88 103 160 167 132 95 59 63 15
2020/2021496 43 39 44 43 11 65 19 49 42 69 26 46
2021/2022387 15 39 50 5 4 7 20 28 9 9 109 92
2022/2023952 73 214 28 111 68 161 110 49 91 9 26 12
2023/2024238 15 31 51 19 24 9 11 61 4 3 10 0
Totale 3.962